Data / Medical devices / Board, Bed
Board, Bed (FPS): 7 FDA-registered makers in 4 countries
7 establishments in 4 countries are registered with the FDA to make Board, Bed (product code FPS, Class 1, 21 CFR 880.6070). 0 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 1 510(k) clearance under this code, the latest on February 28, 1978, and lists 2 recall events (0 Class I). FDA data exported November 3, 2026.
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- Product code
- FPS
- Device class
- 1
- Regulation
- 880.6070
- Medical specialty
- General Hospital
Makers by country
| Country | Makers |
|---|---|
| China | 3 |
| Taiwan | 2 |
| United Kingdom | 1 |
| Mexico | 1 |
Makers of Board, Bed
Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Hebei Junlaole Medical Technology Co.,ltd | Hengshui City Hebei, China | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Jiangyin Huashi Medical Equipment Co.,Ltd | Jiangyin City Jiangsu, China | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| New Allied Corporation | Taichung City, Taiwan | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Rexyn Ltd | Prescot Liverpool, United Kingdom | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Rogers Foam Tijuana S. de R.L. de C.V. | Tijuana Baja California, Mexico | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Valentine Intl. Ltd. | Hsichih City, Taipei Hsien, Taiwan | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Zhongshan Saxin Electric Heating Technology Co., Ltd. | Zhongshan Guangdong, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated February 28, 1978. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.